My Vids epilepsy a
I have temporal lobe epilepsy with frontal lobe abnormalities. I also www. EpilepsySupportGroup. co. United Kingdom experienced information and support for all types of epilepsy, medications, seizures, etc. If you suffer, curious, or simply to help raise awareness of epilepsy. . . please join. Sequences are a series of attacks that have taken place in both the bath and so on the fourth floor in the bathroom arrested in March 2008. My fiance is with me and keep me of course. This video has no sound, because we do not find how it was done. More videos will follow that have to do is sound on them. I condensed matter, there was a lot of this particular event. Please feel free to log on this video with a link to my support group, to distribute. Thank you for your attention. Tania x
This entry was posted by admin on July 18, 2010 at 8:11 am, and is filed under Health Conditions. Follow any responses to this post through RSS 2.0.You can leave a response or trackback from your own site.
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#2 written by backatjapan29 1 year ago
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#3 written by DanielR305 1 year ago
I have temporal lobe epilepsy, and its gone worse over the last year so I have 3 to 8 absent fits a day thankfully not as severe as above but I could talking one min I am next a couple of jolts then I am told I wake up normally 5 or 10 mins later with a headache and also the feeling of feeling hungover and tired also at times I get twitches behind my eyes I feel so alone with it yet I never had any medication for it when I saw the registrar he was amazed I wasn’t on any medication he was cont
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#4 written by DanielR305 1 year ago
I was not any medication for it he said he would get scans done then I would called back for the results I had all tests done they ask for yet I have seen the consultant yet as he retired and there are no other consultant neurologists in the county yet and I have been waiting since April to get my results which I am not impressed by at all I feel I am suffering unnecessary I feel like many failed by the nhs I personally scrap the nhs re build it for 21st century
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#7 written by DJuggz06 1 year ago
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#9 written by CDFoakley 1 year ago
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#10 written by funkyfairyuk 1 year ago
It can be so hard to strike the right balance regarding safety and privacy. Something I can recommend (I know it sounds odd) is a 2 way baby monitor. That way if a seizure occurs you can here it happening and get to him without his loss of privacy. Likewise you can enquire if he’s okay if all goes quiet, and if he’s fine and just relaxing etc he can answer, again without losing privacy.
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#13 written by evensis 1 year ago
My father suffers from seizures but is still aware, but is totally unable to communicate. Frightening thing he was landing an aircraft once while having one (stress is his trigger and was one of the first time’s he had flown solo). This was when he no idea he had a fist sized tumor in his head! 38 trips to the doctors before he got a diagnosis (Shock horror NHS again!). Suffice to say no more flying! 15 years later it hasn’t grown back, cross fingers! thanks for your video!
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#14 written by MrzTwerksomeMan212 1 year ago
@CDFoakley WOW!!! I JUST HAD ONE IN THE BATHROOM LAST WEEK AND YEA IM NOT ALLOWED TO LOCK THE DOORS ANYMORE!!!
But itz was quite interesting; my mother said she told me to open the door, but i answered her and told her i didn’t know the combination, imean does confusion happen?? idk, but it was mad crazy!! -
#16 written by RU5H1NG 1 year ago
Hi There, my partner has TLE, it however does not have the same symptoms as yours – he becomes very aggressive and has psychotic episodes. It took a long time convincing people that it was a neurological problem and not a psychiatric disorder. It is taking a long time to control the seizures, we are both very tired from it all.
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#18 written by mcneile 1 year ago
Thank you for posting this video. It is so wonderful that you have a fiance that is such a support, and take of you. No doctors in my State are willing to diagnose me with epilepsy, and I actually lost my job because of it. I have no health insurance, and not sure where to go to get help; so my life can be normal again. My symptoms looks very similar to yours, so scary.
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#20 written by liltitch81 1 year ago
I am so happy to have found ur video and support site, I had my first seizure on sunday and although its not a good thing to have its just good to know that others are going thru the same. I was conscious through it, well I knew my boyfriend was there and I kept fighting it but I did lose all awareness briefly.
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i had watter on my brain when i was a babey and it showed when i was 14 i had fits and now im on good meds and i have a tube that drains the water in too my tummy. fk all the people who think fits are funny fk them aye. i respect all the cool people in here